Public Release: 

Mechanism for precise targeting of the immune response uncovered

Science publication describes quality control of antigenes

Goethe University Frankfurt

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IMAGE: This is an image of a space-filling model of the solved protein complex responsible for the selection of antigens. view more 

Credit: AG Tampé

FRANKFURT. The immune system monitors the health status of the cells in our bodies by examining a kind of molecular passport. Sometimes cells present the wrong passport, which can lead to autoimmune diseases, chronic inflammation, or cancer. In the new issue of the journal Science (first release), scientists of the Goethe University Frankfurt have now elucidated the mechanism of how the correct molecular passport is selected.

Most cells provide the T cells of the adaptive immune system with information about their condition by presenting selected components of their interior (antigens) on their surface. If these components include fragments of viruses or altered cell components, the affected cell is eliminated by the T cells. The selection of the antigens is crucial in this process. Presenting the wrong antigens leads to either healthy cells being attacked by the immune system - causing autoimmune diseases or chronic inflammation - or to diseased cells not being recognized, allowing cancer cells or virus-infected cells to escape immune surveillance.

Dr. Christoph Thomas and Prof. Robert Tampé from the Institute of Biochemistry at Goethe University have now unraveled on a molecular level how antigens are selected in the cell for presentation on the cell surface. The protein structure they present shows for the first time the kind of quality control antigens undergo to enable a precise and effective immune response.

"Our work solves a 30-year-old problem of cellular immunity, in particular how antigens associated with tumors or pathogens are selected through processes of editing and quality control in order to generate a specific immune response" explains Prof. Robert Tampé the significance of the publication.

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Publication:

Christoph Thomas, Robert Tampé: Structure of the TAPBPR-MHC I complex defines the mechanism of peptide loading and editing, Science (Oct 12, 2017, First Release)

An image for downloading can be found here: (https://www.dropbox.com/s/t4k1u37h01s0p20/TAPBPR_complex_space_filling.png?dl=0)

Figure legend: Space-filling model of the solved protein complex responsible for the selection of antigens

Contacts:

Prof. Dr. Robert Tampé
49-69-798- 29475
tampe@em.uni-frankfurt.de

Dr. Christoph Thomas
c.thomas@em.uni-frankfurt.de
Institute of Biochemistry, Campus Riedberg
Goethe University Frankfurt, Germany

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